“…In addition, 29 known phenolic compounds were obtained and identified by comparison of physical and spectral data with those reported in the literature. The following known phenolic compounds were identified in the CHCl 3 -MeOH (19:1) fraction: echinatin (11, 5.4 mg) [5], lichocalcone B (12, 17.3 mg) [6], morachalcone A (13, 14.1 mg) [7], 2′,3,4′-trihydroxy-3′-γ,γ-dimethylallyl-6′′,6′′-dimethylpyrano[2′′,3′′:4,5]chalcone (14, 17.4 mg) [8], 1-(2′,4′-dihydroxyphenyl)-2-hydroxy-3-(4′′-hydroxyphenyl)-1-propanone (15, 5.8 mg) [9], kanzonol Y (16, 2.5 mg) [10], (3R)-vestitol (17, 10.5 mg) [11], (3R)-2′,3′,7-trihydroxy-4′-methoxyisoflavan (18, 8.1 mg) [12], kanzonol X (19, 37.1 mg) [10], glabridin (20,193 hispaglabridin A (23, 13.7 mg) [14], hispaglabridin B (24, 10.7 mg) [14], glabrene (25, 28.8 mg) [16], kanzonol W (26, 3.0 mg) [10], glabrocoumarin (27,16.4 mg) [17], shinpterocarpin (28,41.0 mg) [18], O-methylshinpterocarpin (29, 32.4 mg) [18], licoagrocarpin (30, 6.1 mg) [19], licoflavanone A (31, 4.8 mg) [20], glabrol (32, 13.5 mg) [13], shinflavanone (33, 7.8 mg) [18], euchrenone a5 (34, 1.5 mg) [21], xambioona (35,8.0 mg) [22], gancaonin L (36, 8.8 mg) [23], glabrone (37, 15.5 mg) [24], kanzonol U (38, 21.6 mg) [11], and 8,8-dimethyl-3,4-dihydro-2H,8H-pyrano[2,3-f]-chromon-3-ol (39, 17.4 mg) [25] (Figure 4). The structures of isolated compounds were classified into 12 groups: chalcones (1-4, 11-16), isoflavans (5, 6, 17-24), an isoflavone (25), 3-arylcoumarins (26, 27), pterocarpans (28-30), a flavone (31), a flava...…”